ISENTRESS - 49349-430-02 - (RALTEGRAVIR)

Alphabetical Index


Drug Information of ISENTRESS

Product NDC: 49349-430
Proprietary Name: ISENTRESS
Non Proprietary Name: RALTEGRAVIR
Active Ingredient(s): 400    mg/1 & nbsp;   RALTEGRAVIR
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ISENTRESS

Product NDC: 49349-430
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022145
Marketing Category: NDA
Start Marketing Date: 20130410

Package Information of ISENTRESS

Package NDC: 49349-430-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-430-02)

NDC Information of ISENTRESS

NDC Code 49349-430-02
Proprietary Name ISENTRESS
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-430-02)
Product NDC 49349-430
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name RALTEGRAVIR
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130410
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name RALTEGRAVIR POTASSIUM
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes HIV Integrase Inhibitors [MoA],Human Immunodeficiency Virus Integrase Strand Transfer Inhibitor [EPC]

Complete Information of ISENTRESS


General Information